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A GC box in the bidirectional promoter is essential for expression of the human dihydrofolate reductase and mismatch repair protein 1 genes.

作者信息

Fujii H, Shinya E, Shimada T

机构信息

Clinical Hematology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

FEBS Lett. 1992 Dec 7;314(1):33-6. doi: 10.1016/0014-5793(92)81455-u.

DOI:10.1016/0014-5793(92)81455-u
PMID:1451803
Abstract

The human dihydrofolate reductase and mismatch repair protein 1 genes are organized in a head-to-head configuration separated by an 88 base-pair segment and directed by a bidirectional promoter. In vivo transient assays of the site directed mutant promoters using firefly luciferase as a reporter showed that an AT-rich sequence, ACAAATA, in the GC-rich promoter sequence is not required for transcription. However, two out of four GC boxes were shown to function as bidirectional positive regulatory elements. Among them, a GC box at the midpoint of the region between the two initiation sites is essential for supporting minimal bidirectional activity.

摘要

相似文献

1
A GC box in the bidirectional promoter is essential for expression of the human dihydrofolate reductase and mismatch repair protein 1 genes.
FEBS Lett. 1992 Dec 7;314(1):33-6. doi: 10.1016/0014-5793(92)81455-u.
2
Identification of two initiator elements in the bidirectional promoter of the human dihydrofolate reductase and mismatch repair protein 1 genes.人二氢叶酸还原酶和错配修复蛋白1基因双向启动子中两个起始元件的鉴定
Nucleic Acids Res. 1994 Jun 11;22(11):2143-9. doi: 10.1093/nar/22.11.2143.
3
Transcriptional regulation of the dihydrofolate reductase/rep-3 locus.二氢叶酸还原酶/rep-3基因座的转录调控
Crit Rev Eukaryot Gene Expr. 1994;4(1):19-53. doi: 10.1615/critreveukargeneexpr.v4.i1.20.
4
Transcriptional initiation is controlled by upstream GC-box interactions in a TATAA-less promoter.转录起始由无TATAA启动子中的上游GC盒相互作用控制。
Mol Cell Biol. 1990 Dec;10(12):6632-41. doi: 10.1128/mcb.10.12.6632-6641.1990.
5
The bidirectionally transcribed dihydrofolate reductase and rep-3a promoters are growth regulated by distinct mechanisms.双向转录的二氢叶酸还原酶和rep - 3a启动子受不同机制调控生长。
Cell Growth Differ. 1995 May;6(5):541-8.
6
A 165-base pair sequence between the dihydrofolate reductase gene and the divergently transcribed upstream gene is sufficient for bidirectional transcriptional activity.二氢叶酸还原酶基因与反向转录的上游基因之间一段165个碱基对的序列足以实现双向转录活性。
J Biol Chem. 1989 Dec 5;264(34):20171-4.
7
Sequences downstream of the transcription initiation site modulate the activity of the murine dihydrofolate reductase promoter.转录起始位点下游的序列调节小鼠二氢叶酸还原酶启动子的活性。
Mol Cell Biol. 1990 Apr;10(4):1390-8. doi: 10.1128/mcb.10.4.1390-1398.1990.
8
Characterization of a mammalian ribosomal protein gene promoter.
Biochem Cell Biol. 1990 Jun;68(6):949-56. doi: 10.1139/o90-140.
9
Escherichia coli Fis and DnaA proteins bind specifically to the nrd promoter region and affect expression of an nrd-lac fusion.大肠杆菌Fis蛋白和DnaA蛋白特异性结合到nrd启动子区域,并影响nrd - lac融合基因的表达。
J Bacteriol. 1994 Jan;176(2):378-87. doi: 10.1128/jb.176.2.378-387.1994.
10
Transcription from TATA-less promoters: dihydrofolate reductase as a model.无TATA框启动子的转录:以二氢叶酸还原酶作为模型
Crit Rev Eukaryot Gene Expr. 1993;3(4):229-54.

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